ENST00000649046.1:c.12253C>T
MANE Select
|
ENSP00000496870.1:p.Gln4085Ter
|
|
ENST00000649153.1:c.3153C>T
|
|
|
ENST00000650252.1:c.1281C>T
|
ENSP00000496887.1:p.Ser427=
|
|
ENST00000263816.7:c.12253C>T
|
ENSP00000263816.3:p.Gln4085Ter
|
|
NM_004525.2:c.12253C>T
|
NP_004516.2:p.Gln4085Ter
|
|
XM_011511183.1:c.12124C>T
|
XP_011509485.1:p.Gln4042Ter
|
|
XM_011511184.1:c.9964C>T
|
XP_011509486.1:p.Gln3322Ter
|
|
NM_004525.3:c.12253C>T
MANE Select
|
NP_004516.2:p.Gln4085Ter
|
|
XM_011511183.3:c.12124C>T
|
XP_011509485.1:p.Gln4042Ter
|
|
XM_011511184.2:c.9964C>T
|
XP_011509486.1:p.Gln3322Ter
|
|